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SMITH & NEPHEW Dyonics 25 Fluid Management System - Indonesia BPOM Medical Device Registration

SMITH & NEPHEW Dyonics 25 Fluid Management System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21301311113. The device is manufactured by SMITH & NEPHEW INC., ENDOSCOPY DIVISION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.

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BPOM Registered
Risk Class Kelas Resiko : B
SMITH & NEPHEW Dyonics 25 Fluid Management System
Analysis ID: AKL 21301311113

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. TAWADA HEALTHCARE

AR Address

Rukan Permata Senayan Blok A18-19 Lantai 5 Jl. Tentara Pelajar No. 5

Registration Date

Sep 05, 2024

Expiry Date

Dec 31, 2027

Product Type

Diagnostic Orthopedic Equipment

Arthroscope.

Non Radiation Electromedics

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